Senior Scientist, Risk Management & Safety Surveillance

📋 Description

• Ensure timely, quality reports/safety analyses related to core deliverables with oversight as
• Collaborate with Therapeutic Area Safety Head (TASH), MSO, Safety Surveillance Physician (SSP) and
• Initiate, conduct, and oversee searches of internal and external databases
• Perform and/or lead aggregate safety analysis and case level review
• Author, contribute, and coordinate the preparation of core safety deliverables
• Ensure commitments (e.g., Pharmacovigilance Agreements (PVAs) and assessment reports) are met

🎯 Requirements

• Bachelor’s degree in Health or Biomedical Science with six to eight years of industry experience
• Physician (MD or equivalent) with 2-5 years of pharmacovigilance experience or other relevant
• Clinical/medical writing or pharmacovigilance experience preferred
• Strong English verbal and written communication skills
• Demonstrated knowledge of principles of drug development, risk/benefit assessment, and global

🎁 Benefits

• Excellent work-life balance
• Professional development opportunities
• Quality-focused, collaborative 'one-team' culture
• Continuous training and development
• Equal opportunity employer, diverse and inclusive workplace
• Below industry average turnover rates